chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187663799276637993CG55GENIChomozygous110409581
187663811976638120CT69GENICpossibly homozygous110870155
187663824876638249AG62GENIChomozygous110409583
187663826676638267CT65GENIChomozygous110409585
187663924376639244CT66GENIChomozygous110409589
187663925276639253TC68GENIChomozygous110409591
187663946676639467TC69GENICpossibly homozygous110409593
187663978576639786TG51GENIChomozygous110409595
187664103976641040TC68GENIChomozygous110409597
187664400876644009CT53GENIChomozygous110409599
187664669176646692TC66GENIChomozygous110870157
187664904276649043CT49GENIChomozygous110409603
187665032676650327AG47GENIChomozygous110732989
187665902076659021TC71GENIChomozygous110870159
187664035376640354GA26GENIChomozygous119502340
187664233976642340TC27GENIChomozygous131762189
187666031276660313A49GENIChomozygous129554769
187666036076660361A52GENIChomozygous129554770
187664495276644952ATGTGTTCTGTGTGCATGC46GENIChomozygous131758423
187664607676646078TT53GENIChomozygous131758424